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Small Nerve Fiber Pathology in Critical Illness
BACKGROUND: Degeneration of intraepidermal nerve fibers (IENF) is a hallmark of small fiber neuropathy of different etiology, whose clinical picture is dominated by neuropathic pain. It is unknown if critical illness can affect IENF. METHODS: We enrolled 14 adult neurocritical care patients with pro...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787101/ https://www.ncbi.nlm.nih.gov/pubmed/24098716 http://dx.doi.org/10.1371/journal.pone.0075696 |
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author | Latronico, Nicola Filosto, Massimiliano Fagoni, Nazzareno Gheza, Laura Guarneri, Bruno Todeschini, Alice Lombardi, Raffaella Padovani, Alessandro Lauria, Giuseppe |
author_facet | Latronico, Nicola Filosto, Massimiliano Fagoni, Nazzareno Gheza, Laura Guarneri, Bruno Todeschini, Alice Lombardi, Raffaella Padovani, Alessandro Lauria, Giuseppe |
author_sort | Latronico, Nicola |
collection | PubMed |
description | BACKGROUND: Degeneration of intraepidermal nerve fibers (IENF) is a hallmark of small fiber neuropathy of different etiology, whose clinical picture is dominated by neuropathic pain. It is unknown if critical illness can affect IENF. METHODS: We enrolled 14 adult neurocritical care patients with prolonged intensive care unit (ICU) stay and artificial ventilation (≥ 3 days), and no previous history or risk factors for neuromuscular disease. All patients underwent neurological examination including evaluation of consciousness, sensory functions, muscle strength, nerve conduction study and needle electromyography, autonomic dysfunction using the finger wrinkling test, and skin biopsy for quantification of IENF and sweat gland innervation density during ICU stay and at follow-up visit. Development of infection, sepsis and multiple organ failure was recorded throughout the ICU stay. RESULTS: Of the 14 patients recruited, 13 (93%) had infections, sepsis or multiple organ failure. All had severe and non-length dependent loss of IENF. Sweat gland innervation was reduced in all except one patient. Of the 7 patients available for follow-up visit, three complained of diffuse sensory loss and burning pain, and another three showed clinical dysautonomia. CONCLUSIONS: Small fiber pathology can develop in the acute phase of critical illness and may explain chronic sensory impairment and pain in neurocritical care survivors. Its impact on long term disability warrants further studies involving also non-neurologic critical care patients. |
format | Online Article Text |
id | pubmed-3787101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37871012013-10-04 Small Nerve Fiber Pathology in Critical Illness Latronico, Nicola Filosto, Massimiliano Fagoni, Nazzareno Gheza, Laura Guarneri, Bruno Todeschini, Alice Lombardi, Raffaella Padovani, Alessandro Lauria, Giuseppe PLoS One Research Article BACKGROUND: Degeneration of intraepidermal nerve fibers (IENF) is a hallmark of small fiber neuropathy of different etiology, whose clinical picture is dominated by neuropathic pain. It is unknown if critical illness can affect IENF. METHODS: We enrolled 14 adult neurocritical care patients with prolonged intensive care unit (ICU) stay and artificial ventilation (≥ 3 days), and no previous history or risk factors for neuromuscular disease. All patients underwent neurological examination including evaluation of consciousness, sensory functions, muscle strength, nerve conduction study and needle electromyography, autonomic dysfunction using the finger wrinkling test, and skin biopsy for quantification of IENF and sweat gland innervation density during ICU stay and at follow-up visit. Development of infection, sepsis and multiple organ failure was recorded throughout the ICU stay. RESULTS: Of the 14 patients recruited, 13 (93%) had infections, sepsis or multiple organ failure. All had severe and non-length dependent loss of IENF. Sweat gland innervation was reduced in all except one patient. Of the 7 patients available for follow-up visit, three complained of diffuse sensory loss and burning pain, and another three showed clinical dysautonomia. CONCLUSIONS: Small fiber pathology can develop in the acute phase of critical illness and may explain chronic sensory impairment and pain in neurocritical care survivors. Its impact on long term disability warrants further studies involving also non-neurologic critical care patients. Public Library of Science 2013-09-30 /pmc/articles/PMC3787101/ /pubmed/24098716 http://dx.doi.org/10.1371/journal.pone.0075696 Text en © 2013 Latronico et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Latronico, Nicola Filosto, Massimiliano Fagoni, Nazzareno Gheza, Laura Guarneri, Bruno Todeschini, Alice Lombardi, Raffaella Padovani, Alessandro Lauria, Giuseppe Small Nerve Fiber Pathology in Critical Illness |
title | Small Nerve Fiber Pathology in Critical Illness |
title_full | Small Nerve Fiber Pathology in Critical Illness |
title_fullStr | Small Nerve Fiber Pathology in Critical Illness |
title_full_unstemmed | Small Nerve Fiber Pathology in Critical Illness |
title_short | Small Nerve Fiber Pathology in Critical Illness |
title_sort | small nerve fiber pathology in critical illness |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787101/ https://www.ncbi.nlm.nih.gov/pubmed/24098716 http://dx.doi.org/10.1371/journal.pone.0075696 |
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